Tetrahydrofuran → 2-Ethoxycarbonyl-3-phenethyl-succinic acid diethyl ester

HRID 899071Notes

Reaction equation

HRID 899071 reaction equation
C([C:3](CC)([C:7]([O-:9])=[O:8])[C:4]([O-:6])=[O:5])C.[H-].[Na+].[CH2:14]([O:16][C:17](=[O:40])[CH:18](OS(C1C=CC([N+]([O-])=O)=CC=1)(=O)=O)[CH2:19][CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[CH3:15].CN1C(=O)N(C)[CH2:45][CH2:44]C1.[CH2:50]1COC[CH2:51]1>O>[CH2:50]([O:9][C:7](=[O:8])[CH:3]([C:4]([O:6][CH2:44][CH3:45])=[O:5])[CH:18]([CH2:19][CH2:20][C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1)[C:17]([O:16][CH2:14][CH3:15])=[O:40])[CH3:51]

Participants

7

Procedure

A solution of diethylmalonate (240.2 mg, 1.5 mmol) and NaH (43.2 mg, 1.8 mmol) in THF (3 ml) was stirred for one hour at room temperature under argon. 2-(4-Nitro-benzenesulfonyloxy)-4-phenyl-butyric acid ethyl ester (590 mg, 1.5 mmol) and DMPU (192.2 mg, 1.5 mmol) was added and the mixture was stirred at room temperature for three days. The reaction was poured into H2O and extracted with ethyl acetate. The organic layer was washed with water and concentrated under reduced pressure. The product was purified by column chromatography (petroleumether/ethyl acetate, 4:1) to give 2-ethoxycarbonyl-3-phenethyl-succinic acid diethyl ester (274 mg, 52.1%).

Workup

  1. extractionextracted with ethyl acetate
  2. washThe organic layer was washed with water
  3. concentrationconcentrated under reduced pressure
  4. customThe product was purified by column chromatography (petroleumether/ethyl acetate, 4:1)

Sources & evidence

ORD record
ord-2d3f5065d0644036997ed11b400c7493
Source dataset
uspto-grants-2008_04
Patent number
US07354895B1

Reaction notes

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